Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease

Author(s)

    • ROGAEVA Ekaterina
    • Centre for Research in Neurodegenerative Diseases and Toronto Western Hospital, Division of Neurology, Department of Medicine, University of Toronto
    • MURAYAMA Shigeo
    • Department of Geriatric Neuroscience (Neuropathology), Tokyo Metropolitan Institute of Gerontology
    • MARRAS Connie
    • Division of Neurology University Health Network, Department of Medicine, Movement Disorders Centre, Toronto Western Hospital
    • LANG Anthony E
    • Division of Neurology University Health Network, Department of Medicine, Movement Disorders Centre, Toronto Western Hospital
    • GEORGE-HYSLOP Peter St
    • Centre for Research in Neurodegenerative Diseases and Toronto Western Hospital, Division of Neurology, Department of Medicine, University of Toronto
    • GOTO Jun
    • Department of Neurology, Graduate School of Medicine, University of Tokyo
    • TSUJI Shoji
    • Department of Neurology, Graduate School of Medicine, University of Tokyo

Journal

  • Journal of human genetics

    Journal of human genetics 56(9), 671-675, 2011-09-01

    Nature Publishing Group

References:  46

Codes

  • NII Article ID (NAID)
    10030660937
  • NII NACSIS-CAT ID (NCID)
    AA11206160
  • Text Lang
    ENG
  • Article Type
    ART
  • ISSN
    14345161
  • NDL Article ID
    11245408
  • NDL Source Classification
    ZS16(科学技術--医学--人類遺伝学)
  • NDL Call No.
    Z54-H248
  • Data Source
    CJP  NDL 
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